DIN EN ISO 1135-5 Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015)
Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- IEC 62471 Photobiological safety of lamps and lamp systems - Edition 1.0
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- 59
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- IEC 62471 Photobiological safety of lamps and lamp systems - Edition 1.0
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- 59.040
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- IEC 62471 Photobiological safety of lamps and lamp systems - Edition 1.0
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- 97
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- IEC 62471 Photobiological safety of lamps and lamp systems - Edition 1.0
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- 97.140
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- IEC 62471 Photobiological safety of lamps and lamp systems - Edition 1.0
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- CEN EN 13855-2 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 2: Test method by oscillation
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- IEC 62471 Photobiological safety of lamps and lamp systems - Edition 1.0
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- CEI EN 61496-2 Safety of machinery - Electro-sensitive protective equipment Part 2: Particular requirements for equipment using active opto-electronic protective devices (AOPDs)
- IEC 62471 Photobiological safety of lamps and lamp systems - Edition 1.0
- ISO 16142-1 Medical devices - Recognized essential principles of safety and performance of medical devices - Part 1: General essential principles and additional specific essential principles for all non?IVD medical devices and guidance on the selection of standards - First Edition
- ISO 7864 Sterile hypodermic needles for single use - Requirements and test methods - Fourth Edition
- CEN EN 13855-1 Manufactured articles solely filled with feathers and down - Measurement of thickness and compressibility of cushions - Part 1: Test method by rotation
- Картотека зарубежных и международных стандартов
Deutsches Institut fur Normung e. V.
Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015)
N EN ISO 1135-5
Annotation
This part of ISO 1135 specifies requirements for single use transfusion sets for use with pressure infusion equipment capable of generating pressures up to 200 kPa (2 bar). This International Standard ensures compatibility with containers for blood and blood components as well as intravenous equipment.
Secondary aims of this part of ISO 1135 are to provide guidance on specifications relating to the quality and performance of materials used in transfusion sets, to present designations for transfusion set components, and to ensure the compatibility of sets with red cell and plasma blood components.
Platelet components should not be transfused under pressure using these sets.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over this part of ISO 1135.
Автоматический перевод:
Оборудование для переливания для медицинского использования - Часть 5: Переливание устанавливает для единственного использования с инфузионным прибором давления (1135-5:2015 ISO)
Эта часть ISO 1135 определяет требования для единственных наборов переливания использования для использования с оборудованием вливания давления, способным к генерации давлений до 200 кПа (2 пластинки). Этот Международный стандарт гарантирует совместимость контейнерами для компонентов крови и крови, а также внутривенного оборудования.



